Background: There is preliminary evidence linking physical activity to better prostate cancer outcomes, though the molecular mechanisms underlying this association are not clear.
Methods: In a Seattle-based cohort of patients diagnosed with clinically localized prostate cancer and prospective follow-up for outcomes ( = 1,354), we studied the association between self-reported vigorous physical activity and prostate cancer progression to a metastatic-lethal phenotype. A subset of patients had prostate cancer tissue samples available for investigating DNA methylation (Infinium HumanMethylation450 BeadChip array) and exercise ( = 524).
Results: Patients who had vigorous physical activity at least once per week during the year before diagnosis (∼79% of the cohort) were significantly less likely to progress to metastatic-lethal prostate cancer compared with those who had vigorous physical activity less frequently (adjusted hazard ratio = 0.63; = 0.029). Among the subset of men who had radical prostatectomy as primary treatment and tumor tissue available, a differentially methylated region (DMR) was identified (family-wise error rate = 0.03, hypomethylated in the weekly exercise group), with 9 methylation probes located in the promoter region of . This gene encodes a calcium binding protein involved in innate immune response. The methylation level of the nine CpGs was inversely correlated with gene expression (average correlation coefficient = -0.35).
Conclusions: Vigorous physical activity before diagnosis is associated with epigenetic alterations of and prostate cancer metastatic-lethal progression.
Impact: This analysis provides strong evidence for the association between vigorous physical activity and a less likelihood to develop metastatic-lethal progression, and a suggestive link between exercise and DNA methylation in the gene.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363836 | PMC |
http://dx.doi.org/10.1158/1055-9965.EPI-18-0622 | DOI Listing |
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